Anaplastic Large Cell Lymphoma Associated With Breast Implants: A Report of 13 Cases

被引:124
作者
Aladily, Tariq N.
Medeiros, L. Jeffrey
Amin, Mitual B. [2 ]
Haideri, Nisreen [3 ]
Ye, Dongjiu [4 ]
Azevedo, Sergio J. [6 ]
Jorgensen, Jeffrey L.
de Peralta-Venturina, Mariza [5 ]
Mustafa, Eid B. [8 ]
Young, Ken H.
You, M. James
Fayad, Luis E. [7 ]
Blenc, Ann Marie [2 ]
Miranda, Roberto N. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Unit 072, Houston, TX 77030 USA
[2] Oakland Univ, Dept Pathol, William Beaumont Sch Med, Royal Oak, MI USA
[3] Univ Kansas, Ctr Canc, Dept Hematol & Oncol, Kansas City, KS USA
[4] Bioreference Labs Inc, Dept Pathol, Elmwood Pk, NJ USA
[5] Cedars Sinai Med Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90048 USA
[6] Univ Fed Rio Grande do Sul, Inst Cancer Mae Deus, Sch Med, Dept Med, Porto Alegre, RS, Brazil
[7] Univ Texas MD Anderson Canc Ctr, Dept Lymphoma & Myeloma, Houston, TX 77030 USA
[8] Dept Plast & Reconstruct Surg, Wichita Falls, TX USA
关键词
breast implant-associated ALCL; anaplastic large cell lymphoma; non-Hodgkin lymphoma; OF-THE-LITERATURE; CAPSULE; PATIENT; RECONSTRUCTION; ENTITY; CANCER;
D O I
10.1097/PAS.0b013e31825749b1
中图分类号
R36 [病理学];
学科分类号
100103 [病原生物学];
摘要
We report 13 cases of anaplastic large cell lymphoma (ALCL) associated with breast implants. Patient age ranged from 39 to 68 years, and the interval from implant to ALCL was 4 to 29 years. All tumors were composed of large, pleomorphic cells that were CD30(+) and ALK1(-), and all 7 cases assessed had monoclonal T-cell receptor gamma-chain rearrangements. Two patient subgroups were identified. Ten patients presented with effusion surrounded by fibrous capsule without a grossly identifiable tumor mass. Nine patients had stage I and 1 had stage II disease. Eight patients underwent implant removal and capsulectomy. Four patients received chemotherapy and 4 radiation therapy. All patients were alive without disease at last follow-up. A second subgroup of 3 patients had effusion and a distinct mass adjacent to the implant. One patient had stage I and 2 stage II disease. One patient had a 3-year history of lymphomatoid papulosis, and 1 patient had a 1-year history of CD30(+) T-cell lymphoma adjacent to the breast before the diagnosis of ALCL associated with breast implant. Two patients received chemotherapy and 1 radiation therapy. Two patients died 2 and 12 years after diagnosis, respectively. We conclude that the clinical behavior of ALCL associated with breast implants is heterogeneous. Patients who present with effusion without a distinct mass have an indolent disease course, similar to CD30(+) lymphoproliferative disorder of skin. In contrast, patients who present with a distinct mass may have advanced stage or possibly systemic disease and have a poorer prognosis.
引用
收藏
页码:1000 / 1008
页数:9
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